Search
for
Sort by
Research 31–60 of 1000+
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- Estrogen modulates mesenchymal-epidermal interactions in the adult nipple
- Vitamin D, Lipid Metabolism and Prostate Cancer
- Deciphering the cellular landscape and genetic underpinnings of fiber diameter determined by dermal papilla cells in fine-wool sheep
- Mendelian Randomization Identifies CD25+ CD4+ Tregs and Plasma Proteins in Androgenetic Alopecia Pathogenesis
- Progress on genome-wide association studies and selection signature analysis for agronomic traits in Chinese sheep and goats: review
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- Natural Killer Group 2 Type D (NKG2D) Gene Polymorphism in Systemic Lupus Erythematosus-Suez Canal Region - Egypt
- Abstracts
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk
- Male Pattern Baldness in Relation to Prostate Cancer–Specific Mortality: A Prospective Analysis in the NHANES I Epidemiologic Follow-up Study
- Potential genetic associations of acne scar phenotypes: IL1A in fibrotic scarring and CYB5R1 in atrophic scarring
- Genetic prediction of male pattern baldness
- COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine
- Morpho-Regulation of Ectodermal Organs
- MicroRNA-214 controls skin and hair follicle development by modulating the activity of the Wnt pathway
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Conditional knock out of N-WASP in keratinocytes causes skin barrier defects and atopic dermatitis-like inflammation
- A role for the Tgf-β/Bmp co-receptor Endoglin in the molecular oscillator that regulates the hair follicle cycle
- The endocrinology of baldness
- Uncovering the complex relationship between balding, testosterone and skin cancers in men
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- Steroid 5α-reductase 2 deficiency leads to reduced dominance-related and impulse-control behaviors
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3